The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.4020-99-9, Name is Methoxydiphenylphosphine, molecular formula is C13H13OP. In a Article，once mentioned of 4020-99-9, Product Details of 4020-99-9
In sharp contrast to tetraphenyldiphosphine, which does not add to carbon?carbon double bonds efficiently, its monoxide, [Ph2P(O)PPh2] can engage in a radical addition to various alkenes, thus affording the corresponding 1-phosphinyl-2-phosphinoalkanes regioselectively, and they can be converted into their sulfides by treatment with elemental sulfur. The phosphinylphosphination proceeds by the homolytic cleavage of the PV(O)?PIIIsingle bond of Ph2P(O)PPh2, followed by selective attack of the phosphinyl radical at the terminal position of the alkenes, and selective trapping of the resulting carbon radical by the phosphino group. Furthermore, the phosphinylphosphination product could be converted directly into its platinum complex with a hemilabile P,O chelation.
Note that a catalyst decreases the activation energy for both the forward and the reverse reactions and hence accelerates both the forward and the reverse reactions.Product Details of 4020-99-9, you can also check out more blogs about4020-99-9
Reference：
Phosphine ligand,
Chiral phosphine ligands in asymmetric synthesis. Molecular structure and absolute configuration of (1,5-cyclooctadiene)-(2S,3S)-2,3-bis(diphenylphosphino)butanerhodium(I) perchlorate tetrahydrofuran solvate